| Year |
Citation |
Score |
| 1996 |
Marcoccia JF, Yates K, Csizmadia IG. An ab initio study on the protonation of formaldoxime in its ground and low-lying valence excited states. A model study for the early steps of acid-catalysed photochemical reactions Journal of Molecular Structure: Theochem. 360: 1-39. DOI: 10.1016/0166-1280(95)04377-2 |
0.331 |
|
| 1990 |
Rachina V, Blagoeva IB, Pojarlieff IG, Yates K. β-Ureido acids and dihydrouracils. The kinetics and mechanism of the reversible ring closure of 3-(3'-methylureido)-propanoic acid and 3-(3-phenylureido)-2-methylpropanoic acid in sulfuric acid solutions Canadian Journal of Chemistry. 68: 1676-1684. DOI: 10.1139/V90-261 |
0.377 |
|
| 1990 |
Sinha HK, Thomson PCP, Yates K. Excited state dipole moments and polarizabilities of some aromatic alkenes and alkynes Canadian Journal of Chemistry. 68: 1507-1513. DOI: 10.1139/V90-232 |
0.317 |
|
| 1989 |
Martin PS, Yates K, Csizmadia IG. A theoretical study of adiabatic proton transfer to simple substituted acetylenes In Their Ground And Excited States Canadian Journal of Chemistry. 67: 2178-2187. DOI: 10.1139/V89-338 |
0.304 |
|
| 1989 |
Yates K. Application of Marcus theory to photochemical proton transfer reactions. II. Modifications based on intersecting state models Journal of Physical Organic Chemistry. 2: 300-322. DOI: 10.1002/Poc.610020403 |
0.359 |
|
| 1988 |
Yates K, Martin P, Csizmadia IG. Theoretical study of acid-catalyzed hydration of ground and excited state acetylenes Pure and Applied Chemistry. 60: 205-207. DOI: 10.1351/Pac198860020205 |
0.347 |
|
| 1988 |
Anderson SW, Yates K. Enhanced nucleophile selectivity in the photoaddition to styrene. Comparison with the thermal addition Canadian Journal of Chemistry. 66: 2412-2421. DOI: 10.1139/V88-380 |
0.309 |
|
| 1987 |
McEwen J, Yates K. Photohydration of styrenes and phenylacetylenes. General acid catalysis and Broensted relationships Journal of the American Chemical Society. 109: 5800-5808. DOI: 10.1021/Ja00253A035 |
0.317 |
|
| 1986 |
Wan P, Yates K. Photoredox chemistry of nitrobenzyl alcohols in aqueous solution. Acid and base catalysis of reaction Canadian Journal of Chemistry. 64: 2076-2086. DOI: 10.1139/V86-343 |
0.352 |
|
| 1986 |
Cox RA, Yates K. Mechanistic studies in strong acids. 11. An excess acidity analysis of acylal and thioacylal hydrolysis in sulfuric acid. Variation of .rho. with acidity Journal of Organic Chemistry. 51: 3619-3624. DOI: 10.1021/Jo00369A013 |
0.322 |
|
| 1986 |
Rafizadeh K, Yates K. Acid-catalyzed photooxidation of m-nitrobenzyl derivatives in aqueous solution Journal of Organic Chemistry. 51: 2777-2781. DOI: 10.1021/Jo00364A029 |
0.303 |
|
| 1986 |
Kalanderopoulos P, Yates K. Intramolecular proton transfer in photohydration reactions Journal of the American Chemical Society. 108: 6290-6295. DOI: 10.1021/Ja00280A028 |
0.32 |
|
| 1984 |
Druet LM, Yates K. Mechanistic variation in the reactions of substituted acetamides in aqueous sulfuric acid Canadian Journal of Chemistry. 62: 2401-2414. DOI: 10.1139/V84-414 |
0.388 |
|
| 1984 |
Cox RA, Yates K. Thermodynamics of protonation of weak bases in H2SO4-H2O media, determined using the excess acidity method Canadian Journal of Chemistry. 62: 2155-2160. DOI: 10.1139/V84-369 |
0.33 |
|
| 1984 |
Cox RA, Yates K. Hydrolysis mechanisms for acylhydrazines in aqueous sulfuric acid, determined using the excess acidity method. Canadian Journal of Chemistry. 62: 1613-1617. DOI: 10.1139/V84-277 |
0.37 |
|
| 1983 |
Cox RA, Yates K. Acidity functions: an update Canadian Journal of Chemistry. 61: 2225-2243. DOI: 10.1139/V83-388 |
0.328 |
|
| 1983 |
Martin PS, Yates K, Csizmadia IG. A theoretical study on the acid catalysed hydration of excited state acetylene Theoretica Chimica Acta. 64: 117-126. DOI: 10.1007/Bf00550326 |
0.359 |
|
| 1982 |
Cox RA, Yates K. Mechanistic studies in strong acids. VIII. Hydrolysis mechanisms for some thiobenzoic acids and esters in aqueous sulfuric acid, determined using the excess acidity method Canadian Journal of Chemistry. 60: 3061-3070. DOI: 10.1139/V82-438 |
0.381 |
|
| 1981 |
Cox RA, Yates K. The hydrolyses of benzamides, methylbenzimidatium ions, and lactams in aqueous sulfuric acid. The excess acidity method in the determination of reaction mechanisms Canadian Journal of Chemistry. 59: 2853-2863. DOI: 10.1139/V81-414 |
0.381 |
|
| 1981 |
Cox RA, Haldna ÜL, Idler KL, Yates K. Resolution of Raman spectra of aqueous sulfuric acid mixtures using principal factor analysis Canadian Journal of Chemistry. 59: 2591-2598. DOI: 10.1139/V81-372 |
0.303 |
|
| 1981 |
Cox RA, Yates K. The excess acidity of aqueous HCl and HBr media. An improved method for the calculation of X-functions and H0 scales Canadian Journal of Chemistry. 59: 2116-2124. DOI: 10.1139/V81-306 |
0.319 |
|
| 1981 |
Cox RA, Druet LM, Klausner AE, Modro TA, Wan P, Yates K. Protonation acidity constants for some benzamides, acetamides, and lactams Canadian Journal of Chemistry. 59: 1568-1573. DOI: 10.1139/V81-231 |
0.34 |
|
| 1981 |
Cox RA, Yates K. Medium effects in protonation equilibrium studies. Accurate acidity constants using the excess acidity method Canadian Journal of Chemistry. 59: 1560-1567. DOI: 10.1139/V81-230 |
0.352 |
|
| 1981 |
Yates K, Mandrapilias G. Vinyl Cation Intermediates In Solvolytic And Electrophilic Reactions. 2. Bromination Of Arylacetylenes Cheminform. 12. DOI: 10.1002/Chin.198102156 |
0.336 |
|
| 1980 |
Wan P, Modro TA, Yates K. The kinetics and mechanism of acid catalysed hydrolysis of lactams Canadian Journal of Chemistry. 58: 2423-2432. DOI: 10.1139/V80-391 |
0.33 |
|
| 1980 |
Yates K, Mandrapilias G. Vinyl cation intermediates in solvolytic and electrophilic reactions. 2. Bromination of arylacetylenes Journal of Organic Chemistry. 45: 3902-3906. DOI: 10.1021/Jo01307A033 |
0.336 |
|
| 1980 |
HOPKINSON AC, LIEN MH, CSIZMADIA IG, YATES K. ChemInform Abstract: QUANTUM CHEMICAL STUDIES ON ELECTROPHILIC ADDITION. IV. REACTION OF THE NITRENIUM ION WITH ETHYLENE AND A COMPARISON OF THE EFFECTIVENESS OF NH2, OH, F, CL AND SH AS BRIDGING SUBSTITUENTS Chemischer Informationsdienst. 11. DOI: 10.1002/Chin.198031073 |
0.305 |
|
| 1979 |
Cox RA, Goldman MF, Yates K. The hydrolyses of some sterically crowded benzoate esters in sulfuric acid. The excess acidity method at different temperatures Canadian Journal of Chemistry. 57: 2960-2966. DOI: 10.1139/V79-481 |
0.355 |
|
| 1979 |
Cox RA, Smith CR, Yates K. The excess acidity method. The basicities, and rates and mechanisms of enolization, of some acetophenones and acetone, in moderately concentrated sulfuric acid Canadian Journal of Chemistry. 57: 2952-2959. DOI: 10.1139/V79-480 |
0.364 |
|
| 1979 |
Cox RA, Yates K. Kinetic equations for reactions in concentrated aqueous acids based on the concept of "excess acidity" Canadian Journal of Chemistry. 57: 2944-2951. DOI: 10.1139/V79-479 |
0.362 |
|
| 1979 |
Modro A, Schmid GH, Yates K. Kinetic solvent isotope effects in the additions of bromine and 4-chlorobenzenesulfenyl chloride to alkenes and alkynes Journal of Organic Chemistry. 11: 4221-4224. DOI: 10.1021/Jo01338A001 |
0.358 |
|
| 1979 |
Cox RA, Krull UJ, Thompson M, Yates K. Acidity functions of aqueous fluorinated acid solutions by differential pulse polarography Analytica Chimica Acta. 106: 51-57. DOI: 10.1016/S0003-2670(01)83703-X |
0.32 |
|
| 1978 |
Cox RA, Yates K. Excess acidities. A generalized method for the determination of basicities in aqueous acid mixtures Journal of the American Chemical Society. 100: 3861-3867. DOI: 10.1021/Ja00480A033 |
0.321 |
|
| 1978 |
Yates K, Modro TA. Transition-state activity coefficients-a new mechanistic tool in the investigation of acid-catalyzed reactions Accounts of Chemical Research. 11: 190-196. DOI: 10.1021/Ar50125A003 |
0.351 |
|
| 1977 |
Hopkinson AC, Lien MH, Yates K, Mezey PG, Csizmadia IG. A nonempirical molecular orbital study on the acidity of the carbon–hydrogen bond The Journal of Chemical Physics. 67: 517-523. DOI: 10.1063/1.434907 |
0.312 |
|
| 1977 |
Altmann JA, Csizmadia IG, Yates K, Yates P. An ab initio study of the rearrangement of carbonyl compounds to oxacarbenes The Journal of Chemical Physics. 66: 298-302. DOI: 10.1063/1.433623 |
0.322 |
|
| 1977 |
Hopkinson AC, Lien MH, Yates K, Csizmadia IG. Quantum chemical studies on electrophilic addition Theoretica Chimica Acta. 44: 385-398. DOI: 10.1007/Bf00547747 |
0.31 |
|
| 1977 |
Altmann JA, Tee OS, Yates K. Application Of The Principle Of Least Motion To Organic Reactions. 4. More Complex Molecular Rearrangements Cheminform. 8. DOI: 10.1002/Chin.197706120 |
0.607 |
|
| 1976 |
Schmid GH, Modro A, Garratt DG, Yates K. The addition of 4-chlorobenzenesulfenyl chloride to phenyl-substituted acetylenes: the structures of the intermediate thiirenium ion Canadian Journal of Chemistry. 54: 3045-3049. DOI: 10.1139/V76-432 |
0.304 |
|
| 1976 |
Modro TA, Reynolds WF, Yates K. Medium effects on tetraalkylammonium ions in aqueous acid solutions Canadian Journal of Chemistry. 54: 1439-1444. DOI: 10.1139/V76-206 |
0.331 |
|
| 1976 |
Schmid GH, Modro A, Lenz F, Garratt DG, Yates K. Reactions of sulfenyl halides and their derivatives. 14. Effect of acetylene structure on the rates and products of addition of 4-chlorobenzenesulfenyl chloride Journal of Organic Chemistry. 41: 2331-2336. DOI: 10.1021/Jo00875A025 |
0.301 |
|
| 1976 |
Altmann JA, Tee OS, Yates K. Application of the principle of least motion to organic reactions. 4. More complex molecular rearrangements Journal of the American Chemical Society. 98: 7132-7138. DOI: 10.1021/Ja00439A003 |
0.607 |
|
| 1976 |
Modro TA, Yates K. Aromatic protodealkylation. Evidence for an A-1 reaction mechanism Journal of the American Chemical Society. 98: 4247-4250. DOI: 10.1021/Ja00430A040 |
0.313 |
|
| 1975 |
McClelland RA, Modro TA, Goldman MF, Yates K. Transition state activity coefficients in the acid-catalyzed hydrolysis of esters Canadian Journal of Chemistry. 55: 3050-3057. DOI: 10.1021/Ja00851A033 |
0.595 |
|
| 1975 |
Mcclelland RA, Modro TA, Goldman MF, Yates K. Transition State Activity Coefficients In The Acid-Catalyzed Hydrolysis Of Esters Cheminform. 6. DOI: 10.1002/Chin.197546183 |
0.563 |
|
| 1974 |
Yates K, McClelland RA. Thermodynamics of Transfer of Organic Molecules from Water to Acid Solutions. The Effects of Nitro Substitution Canadian Journal of Chemistry. 52: 1098-1107. DOI: 10.1139/V74-174 |
0.574 |
|
| 1974 |
Yates K, Perie JJ. Solvolysis of arylvinyl bromides and tosylates Journal of Organic Chemistry. 39: 1902-1908. DOI: 10.1021/Jo00927A024 |
0.312 |
|
| 1974 |
Tee OS, Altmann JA, Yates K. Application of the principle of least motion to organic reactions. III. Eliminations, enolizations, and homoenolizations Journal of the American Chemical Society. 96: 3141-3146. DOI: 10.1021/Ja00817A021 |
0.605 |
|
| 1974 |
Tee OS, Altmann JA, Yates K. Application Of The Principle Of Least Motion To Organic Reactions Part 3, Eliminations, Enolizations, And Homoenolizations Cheminform. 5. DOI: 10.1002/Chin.197429133 |
0.603 |
|
| 1973 |
Yates K, McClelland RA. Hydronium ion activity in strongly acidic media. Remarkable agreement between independent estimates Journal of the American Chemical Society. 95: 3055-3057. DOI: 10.1021/Ja00790A076 |
0.544 |
|
| 1973 |
Yates K, Wai H, Welch G, McClelland RA. Medium dependence of acidity functions and activity coefficients in perchloric acid Journal of the American Chemical Society. 95: 418-426. DOI: 10.1021/Ja00783A018 |
0.553 |
|
| 1973 |
Yates K, Wai H, Welch G, Mcclelland RA. Medium-Abhaengigkeit Von Aciditaetsfunktionen Und Aktivitaetskoeffizienten In Perchlorsaeure Cheminform. 4. DOI: 10.1002/Chin.197329118 |
0.488 |
|
| 1973 |
Yates K, Mcclelland RA. Hydroniumionenaktivitaet In Stark Sauren Medien, Bemerkenswerte Uebereinstimmung Zwischen Unabhaengigen Bestimmungen Cheminform. 4. DOI: 10.1002/Chin.197327025 |
0.505 |
|
| 1972 |
Yates K, Welch G. Acidity Function Behavior in Aqueous-organic Solvents. I. The H0, and HA Functions in 70% DMSO–H2O Canadian Journal of Chemistry. 50: 1513-1522. DOI: 10.1139/V72-239 |
0.302 |
|
| 1972 |
Smith CR, Yates K. Kinetic Evidence for Predominant Oxygen Protonation of Amides Canadian Journal of Chemistry. 50: 771-773. DOI: 10.1139/V72-119 |
0.319 |
|
| 1972 |
Yates K, Shapiro SA. A Critical Test of the Hammett Acidity Function Canadian Journal of Chemistry. 50: 581-583. DOI: 10.1139/V72-089 |
0.319 |
|
| 1972 |
Yates K, Welch G. The Dissociation of Anilinium Ions in Aqueous Dimethylsulfoxide Canadian Journal of Chemistry. 50: 474-478. DOI: 10.1139/V72-073 |
0.306 |
|
| 1972 |
Smith CR, Yates K. Medium And Temperature Dependence Of Acid-Catalyzed Hydrolysis Of N- Methylated Methylbenzimidates And Benzoylimidazole. An Investigation Into The Mechanism Of Amide Hydrolysis. Journal of the American Chemical Society. 94: 8811-8817. DOI: 10.1021/Ja00780A029 |
0.307 |
|
| 1972 |
Tee OS, Yates K. Application of the principle of least motion to organic reactions. II. Molecular rearrangements Journal of the American Chemical Society. 94: 3074-3080. DOI: 10.1021/Ja00764A031 |
0.605 |
|
| 1972 |
Tee OS, Yates K. Anwendung Des Prinzips Der Geringsten Bewegung Auf Organische Rk. 2. Mitt. Molekuelumlagerungen Cheminform. 3. DOI: 10.1002/Chin.197229137 |
0.555 |
|
| 1972 |
YATES K, MCDONALD RS. ChemInform Abstract: THERMOCHEMISCHE UNTERSUCHUNG DES MECHANISMUS DER ELEKTROPHILEN ADDITION VON BROM AN OLEFINE Chemischer Informationsdienst. 3. DOI: 10.1002/Chin.197205108 |
0.469 |
|
| 1971 |
Smith CR, Yates K. Structure, medium, and temperature dependence of acid-catalyzed amide hydrolysis Journal of the American Chemical Society. 93: 6578-6583. DOI: 10.1021/Ja00753A042 |
0.302 |
|
| 1971 |
Yates K, McDonald RS. Thermomechanical probe into the mechanism of electrophilic addition to olefins Journal of the American Chemical Society. 93: 6297-6299. DOI: 10.1021/Ja00752A066 |
0.455 |
|
| 1970 |
Pincock JA, Yates K. Kinetics and mechanism of electrophilic bromination of acetylenes Canadian Journal of Chemistry. 48: 3332-3348. DOI: 10.1139/V70-561 |
0.33 |
|
| 1970 |
Hopkinson AC, Yates K, Csizmadia IG. Ab Initio LCAO–MO–SCF Calculations on Formic Acid, Formate Ion, and Protonated Formic Acid The Journal of Chemical Physics. 52: 1784-1789. DOI: 10.1063/1.1673218 |
0.359 |
|
| 1970 |
Hopkinson A, Yates K, Csizmadia L. Semi-empirical calculations on carbinol—carbonium ion equilibria Tetrahedron. 26: 1845-1857. DOI: 10.1016/S0040-4020(01)92761-9 |
0.307 |
|
| 1969 |
Hopkinson AC, McClelland RA, Yates K, Csizmadia IG. An attempted application of the extended hückel molecular orbital approach to reactions involving charged species Theoretical Chemistry Accounts. 13: 65-78. DOI: 10.1007/Bf00527320 |
0.576 |
|
| 1967 |
Yates K, Wright WV. Kinetics and mechanism of bromination of styrenes Canadian Journal of Chemistry. 45: 167-173. DOI: 10.1139/V67-033 |
0.315 |
|
| 1967 |
Yates K, McClelland RA. Mechanisms of ester hydrolysis in aqueous sulfuric acids Journal of the American Chemical Society. 89: 2686-2692. DOI: 10.1021/Ja00987A033 |
0.578 |
|
| 1964 |
Yates K, Wai H. A Redetermination and Extension of the H0 Scale of Acidity in Aqueous Perchloric Acid Journal of the American Chemical Society. 86: 5408-5413. DOI: 10.1021/Ja01078A008 |
0.301 |
|
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